检索结果 - Day-Williams, Aaron G

The effect of next-generation sequencing technology on complex trait research 由 Day-Williams, Aaron G, Zeggini, Eleftheria

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ARIEL and AMELIA: Testing for an Accumulation of Rare Variants Using Next-Generation Sequencing Data 由 Asimit, Jennifer L., Day-Williams, Aaron G., Morris, Andrew P., Zeggini, Eleftheria

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CCRaVAT and QuTie - enabling analysis of rare variants in large-scale case control and quantitative trait association studies 由 Lawrence, Robert, Day-Williams, Aaron G, Elliott, Katherine S, Morris, Andrew P, Zeggini, Eleftheria

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Linkage Analysis without Defined Pedigrees 由 Day-Williams, Aaron G., Blangero, John, Dyer, Thomas D., Lange, Kenneth, Sobel, Eric M.

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Genome-Wide Association Analysis of Imputed Rare Variants: Application to Seven Common Complex Diseases 由 Mägi, Reedik, Asimit, Jennifer L, Day-Williams, Aaron G, Zeggini, Eleftheria, Morris, Andrew P

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Unifying Ideas for Non-Parametric Linkage Analysis 由 Day-Williams, Aaron G., Blangero, John, Dyer, Thomas D., Lange, Kenneth, Sobel, Eric M.

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GLIDERS - A web-based search engine for genome-wide linkage disequilibrium between HapMap SNPs 由 Lawrence, Robert, Day-Williams, Aaron G, Mott, Richard, Broxholme, John, Cardon, Lon R, Zeggini, Eleftheria

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PINES: phenotype-informed tissue weighting improves prediction of pathogenic noncoding variants 由 Bodea, Corneliu A., Mitchell, Adele A., Bloemendal, Alex, Day-Williams, Aaron G., Runz, Heiko, Sunyaev, Shamil R.

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An Evaluation of Different Target Enrichment Methods in Pooled Sequencing Designs for Complex Disease Association Studies 由 Day-Williams, Aaron G., McLay, Kirsten, Drury, Eleanor, Edkins, Sarah, Coffey, Alison J., Palotie, Aarno, Zeggini, Eleftheria

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Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson’s disease 由 Leonard, Hampton, Blauwendraat, Cornelis, Krohn, Lynne, Faghri, Faraz, Iwaki, Hirotaka, Ferguson, Glen, Day-Williams, Aaron G., Stone, David J., Singleton, Andrew B., Nalls, Mike A., Gan-Or, Ziv

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Large-scale association analysis of TNF/LTA gene region polymorphisms in type 2 diabetes 由 Boraska, Vesna, Rayner, Nigel W, Groves, Christopher J, Frayling, Timothy M, Diakite, Mahamadou, Rockett, Kirk A, Kwiatkowski, Dominic P, Day-Williams, Aaron G, McCarthy, Mark I, Zeggini, Eleftheria

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Radiographic endophenotyping in hip osteoarthritis improves the precision of genetic association analysis 由 Panoutsopoulou, Kalliope, Thiagarajah, Shankar, Zengini, Eleni, Day-Williams, Aaron G, Ramos, Yolande FM, Meessen, Jennifer MTA, Huetink, Kasper, Nelissen, Rob GHH, Southam, Lorraine, Rayner, N William, Doherty, Michael, Meulenbelt, Ingrid, Zeggini, Eleftheria, Wilkinson, J Mark

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A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica 由 Estrada, Karol, Whelan, Christopher W., Zhao, Fengmei, Bronson, Paola, Handsaker, Robert E., Sun, Chao, Carulli, John P., Harris, Tim, Ransohoff, Richard M., McCarroll, Steven A., Day-Williams, Aaron G., Greenberg, Benjamin M., MacArthur, Daniel G.

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Investigation of Association Between Hip Osteoarthritis Susceptibility Loci and Radiographic Proximal Femur Shape 由 Lindner, Claudia, Thiagarajah, Shankar, Wilkinson, J. Mark, Panoutsopoulou, Kalliope, Day‐Williams, Aaron G., Cootes, Timothy F., Wallis, Gillian A., Loughlin, John, Arden, Nigel, Birrell, Fraser, Carr, Andrew, Chapman, Kay, Deloukas, Panos, Doherty, Michael, McCaskie, Andrew, Ollier, William E. R., Rai, Ashok, Ralston, Stuart H., Spector, Timothy D., Valdes, Ana M., Wallis, Gillian A., Mark Wilkinson, J., Zeggini, Eleftheria

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Phenome-wide association studies across large population cohorts support drug target validation 由 Diogo, Dorothée, Tian, Chao, Franklin, Christopher S., Alanne-Kinnunen, Mervi, March, Michael, Spencer, Chris C. A., Vangjeli, Ciara, Weale, Michael E., Mattsson, Hannele, Kilpeläinen, Elina, Sleiman, Patrick M. A., Reilly, Dermot F., McElwee, Joshua, Maranville, Joseph C., Chatterjee, Arnaub K., Bhandari, Aman, Nguyen, Khanh-Dung H., Estrada, Karol, Reeve, Mary-Pat, Hutz, Janna, Bing, Nan, John, Sally, MacArthur, Daniel G., Salomaa, Veikko, Ripatti, Samuli, Hakonarson, Hakon, Daly, Mark J., Palotie, Aarno, Hinds, David A., Donnelly, Peter, Fox, Caroline S., Day-Williams, Aaron G., Plenge, Robert M., Runz, Heiko

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Diagnosis of Parkinson’s disease on the basis of clinical–genetic classification: a population-based modelling study 由 Nalls, Mike A., McLean, Cory Y., Rick, Jacqueline, Eberly, Shirley, Hutten, Samantha J., Gwinn, Katrina, Sutherland, Margaret, Martinez, Maria, Heutink, Peter, Williams, Nigel, Hardy, John, Gasser, Thomas, Brice, Alexis, Price, T. Ryan, Nicolas, Aude, Keller, Margaux F., Molony, Cliona, Gibbs, J. Raphael, Chen-Plotkin, Alice, Suh, Eunran, Letson, Christopher, Fiandaca, Massimo S., Mapstone, Mark, Federoff, Howard J., Noyce, Alastair J, Morris, Huw, Van Deerlin, Vivianna M., Weintraub, Daniel, Zabetian, Cyrus, Hernandez, Dena G., Lesage, Suzanne, Mullins, Meghan, Conley, Emily Drabant, Northover, Carrie, Frasier, Mark, Marek, Ken, Day-Williams, Aaron G., Stone, David J., Ioannidis, John P. A., Singleton, Andrew B.

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A Variant in MCF2L Is Associated with Osteoarthritis 由 Day-Williams, Aaron G., Southam, Lorraine, Panoutsopoulou, Kalliope, Rayner, Nigel W., Esko, Tonu, Estrada, Karol, Helgadottir, Hafdis T., Hofman, Albert, Ingvarsson, Throvaldur, Jonsson, Helgi, Keis, Aime, Kerkhof, Hanneke J.M., Thorleifsson, Gudmar, Arden, Nigel K., Carr, Andrew, Chapman, Kay, Deloukas, Panos, Loughlin, John, McCaskie, Andrew, Ollier, William E.R., Ralston, Stuart H., Spector, Timothy D., Wallis, Gillian A., Wilkinson, J. Mark, Aslam, Nadim, Birell, Fraser, Carluke, Ian, Joseph, John, Rai, Ashok, Reed, Mike, Walker, Kirsten, Doherty, Sally A., Jonsdottir, Ingileif, Maciewicz, Rose A., Muir, Kenneth R., Metspalu, Andres, Rivadeneira, Fernando, Stefansson, Kari, Styrkarsdottir, Unnur, Uitterlinden, Andre G., van Meurs, Joyce B.J., Zhang, Weiya, Valdes, Ana M., Doherty, Michael, Zeggini, Eleftheria

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Genetic risk of Parkinson disease and progression:: An analysis of 13 longitudinal cohorts 由 Iwaki, Hirotaka, Blauwendraat, Cornelis, Leonard, Hampton L., Liu, Ganqiang, Maple-Grødem, Jodi, Corvol, Jean-Christophe, Pihlstrøm, Lasse, van Nimwegen, Marlies, Hutten, Samantha J., Nguyen, Khanh-Dung H., Rick, Jacqueline, Eberly, Shirley, Faghri, Faraz, Auinger, Peggy, Scott, Kirsten M., Wijeyekoon, Ruwani, Van Deerlin, Vivianna M., Hernandez, Dena G., Day-Williams, Aaron G., Brice, Alexis, Alves, Guido, Noyce, Alastair J., Tysnes, Ole-Bjørn, Evans, Jonathan R., Breen, David P., Estrada, Karol, Wegel, Claire E., Danjou, Fabrice, Simon, David K., Ravina, Bernard, Toft, Mathias, Heutink, Peter, Bloem, Bastiaan R., Weintraub, Daniel, Barker, Roger A., Williams-Gray, Caroline H., van de Warrenburg, Bart P., Van Hilten, Jacobus J., Scherzer, Clemens R., Singleton, Andrew B., Nalls, Mike A.

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Genomewide Association Study of Parkinson’s Disease Clinical Biomarkers in 12 Longitudinal Patients’ Cohorts 由 Iwaki, Hirotaka, Blauwendraat, Cornelis, Leonard, Hampton L., Kim, Jonggeol J., Liu, Ganqiang, Maple-Grødem, Jodi, Corvol, Jean-Christophe, Pihlstrøm, Lasse, van Nimwegen, Marlies, Hutten, Samantha J., Nguyen, Khanh-Dung H., Rick, Jacqueline, Eberly, Shirley, Faghri, Faraz, Auinger, Peggy, Scott, Kirsten M., Wijeyekoon, Ruwani, Van Deerlin, Vivianna M., Hernandez, Dena G., Gibbs, J. Raphael, Chitrala, Kumaraswamy Naidu, Day-Williams, Aaron G., Brice, Alexis, Alves, Guido, Noyce, Alastair J., Tysnes, Ole-Bjørn, Evans, Jonathan R., Breen, David P., Estrada, Karol, Wegel, Claire E., Danjou, Fabrice, Simon, David K., Andreassen, Ole, Ravina, Bernard, Toft, Mathias, Heutink, Peter, Bloem, Bastiaan R., Weintraub, Daniel, Barker, Roger A., Williams-Gray, Caroline H., van de Warrenburg, Bart P., Van Hilten, Jacobus J., Scherzer, Clemens R., Singleton, Andrew B., Nalls, Mike A.

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Differences in the Presentation and Progression of Parkinson’s Disease by Sex 由 Iwaki, Hirotaka, Blauwendraat, Cornelis, Leonard, Hampton L., Makarious, Mary B., Kim, Jonggeol J., Liu, Ganqiang, Maple-Grødem, Jodi, Corvol, Jean-Christophe, Pihlstrøm, Lasse, van Nimwegen, Marlies, Smolensky, Luba, Amondikar, Ninad, Hutten, Samantha J., Frasier, Mark, Nguyen, Khanh-Dung H., Rick, Jacqueline, Eberly, Shirley, Faghri, Faraz, Auinger, Peggy, Scott, Kirsten M., Wijeyekoon, Ruwani, Van Deerlin, Vivianna M., Hernandez, Dena G., Gibbs, Raphael J., Day-Williams, Aaron G., Brice, Alexis, Alves, Guido, Noyce, Alastair J., Tysnes, Ole-Bjørn, Evans, Jonathan R., Breen, David P., Estrada, Karol, Wegel, Claire E., Danjou, Fabrice, Simon, David K., Andreassen, Ole A., Ravina, Bernard, Toft, Mathias, Heutink, Peter, Bloem, Bastiaan R., Weintraub, Daniel, Barker, Roger A., Williams-Gray, Caroline H., van de Warrenburg, Bart P., Van Hilten, Jacobus J., Scherzer, Clemens R., Singleton, Andrew B., Nalls, Mike A.

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